FDAFDA · Food and drugs·Recall number D-1173-2017
Procrit (epoetin alfa), 10,000 units/mL, packaged in a) box of 6 single use 1 mL vials (NDC 59676-310-01), b) box of 25 single use 1 mL vials (NDC 59676-310-02), Rx Only, Manufactured by: Amgen, Inc. Thousand Oaks, CA 91320, Manufactured for: Janssen Products, LP Horsham, PA 19044
Published September 27, 2017 · Recall initiated: September 13, 2017
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Presence of particulate matter: glass flakes identified as lamellae observed during a routine quality inspection.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- PROCRIT
- Manufacturer
- Amgen, Inc.
- Distributor
- U.S.A. Nationwide
- Lot
- Lot #: a) G290530A, Exp 07/18; b) G290531A, Exp 07/18
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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